CCN3 and CCN3 peptides and analogs thereof for therapeutic use

ABSTRACT

The present invention provides a method for treating a human patient with a pathology by administering to the subject an effective amount of an agent selected from the group of: native full-length CCN3 proteins; analog CCN3 full-length proteins with native cysteine residues substituted by a replacement amino acid; CCNp native peptide fragments having from about 12 to about 20 amino acids; analog CCNp peptide fragments with native cysteine residues substituted with a replacement amino acid; and combinations thereof.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation of U.S. patent application Ser. No.14/821,494, filed Aug. 7, 2015, now U.S. Pat. No. 10,351,608, which isdivisional of U.S. patent application Ser. No. 13/725,658 filed Dec. 21,2012, now U.S. Pat. No. 9,114,112 issued Aug. 25, 2015, which is acontinuation-in-part of U.S. patent application Ser. No. 13/079,693filed Apr. 4, 2011, now U.S. Pat. No. 8,518,395 issued Aug. 27, 2013,which claims priority to U.S. Provisional Patent Application Ser. No.61/341,694 filed on Apr. 2, 2010, the entirety of each application isincorporated herein by reference and made a part hereof.

FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not Applicable.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has beensubmitted in ASCII format via EFS-Web and is hereby incorporated byreference in its entirety. Said ASCII copy, created on Aug. 7, 2015, isnamed 295792-007512_SL.txt and is 33,565 bytes in size.

BACKGROUND OF THE INVENTION Field of the Invention

The present invention discloses the role of CCN3 in diseases associatedwith the overexpression of CCN2, which include but are not limited tofibrosis, wound healing and cancer. More particularly, the presentinvention discloses CCN3 peptides and analogs designed to the functionof full-length CCN3 proteins for use in achieving enhanced anti-fibroticactivity thereby blocking fibrosis and or scar development, and fortreating cancer and other disease processes where CCN3 and CCN2 areimportant, and in some cases without unwanted effects of the completeCCN3. The isolated and purified, or synthesized CCN3 peptides andspecific analogs are potentially useful in the prevention and/ortreatment of diseases by regulating the expression and/or activity ofCCN2, CCN3 and other CCN-related proteins, as well as collagen and otherextracellular matrix proteins.

The CCN Family of Genes and Proteins

The CCN family of genes presently consists of six distinct members thatencode proteins that participate in fundamental biological processessuch as cell proliferation, attachment, migration, embryogenesis,differentiation, wound healing, angiogenesis, and several pathologies,including fibrosis and tumorigensis. Proteins encoded by the members ofthe CCN gene family are primarily 30-40 kDa proteins and are extremelyrich in cysteine (10% by mass) (Perbal B., NOV and the CCN family ofgenes: structural and functional issues. Molecular Pathology 54: 57-79,2001). More recently, it has been reported that some forms of the CCNproteins (CCN3 included) are in the 35-55 kDa range. They are designatedas cysteine-rich 61 (CYR-61) proteins, connective tissue growth factor(CTGF) proteins, nephroblastoma overexpressed (NOV) proteins,Wnt-induced secreted proteins-1 (WISP-1), Wnt-induced secretedproteins-2 (WISP-2), and Wnt-induced secreted proteins-3 (WISP-3). Morerecently, new nomenclature for this family of genes and proteins hasbeen proposed (see Table 1).

TABLE 1 Proposed Names and Names Currently and Previously Used for CCNFamily of Genes and Proteins Proposed name Names used currently orpreviously CCN1 CYR61 (human, mouse, xenopus), CEF10 (chicken),IGFBP-rP4 (human), βIG-M1 (mouse), CTGF-2, IGFBP10 (human), angioproCCN2 CTGF (human, mouse, chicken, xenopus), βIG-M2 (mouse), FISP12(mouse), IGFBP-rP2 (human), Hsc24 (human), IGFBP8 (human), HBGF-0.8,ecogenin (human) CCN3 NOV (human, rat, chicken, mouse, quail), IGFBP-rP3(human), IGFBP9 (human), NOVH (human), NOVm, mNOV (mouse), xNOV(xenopus) CCN4 WISP-1 (human), ELM-1 CCN5 WISP-2 (human), CTGF-L,CTGF-3, HICP, rCOP-1 (rat) CCN6 WISP-3 (human)

FIG. 1 shows the modular structure of the CCN proteins, in a verysimplistic and linear manner. Although they have a quite conservedmultimodular organization, with four modules sharing identity withinsulin-like growth factor binding proteins (IGFBPs), Von Willebrandfactor (VWC), thrombospondin-1 (TSP1), and a cysteine knot (CT)containing family of growth regulators, the CCN proteins havedistinctive biological properties, are differentially regulated, and donot have complete, 100% homology with each other when amino acidsequences are compared. Their involvement has been shown in multipleorgan systems. One organ that has been the focus of a large number ofstudies is the kidney. The underlying mechanisms of action of CCNproteins are still incompletely understood. Attempts to identify uniquespecific high-affinity signal transducing receptors have been difficult.(Brigstock D. R., Regulation of angiogenesis and endothelial cellfunction by connective tissue growth factor. FEBS Letters 327: 125-130,2003). However, a number of potential receptors for signaling eachperhaps responsible for different activities or functions, have now beententatively identified (Mason, R., Connective tissue growth factor(CCN2), a pathogenic factor in diabetic nephropathy. What does it do?How does it do it? J. Cell Commun. Signal 3: 95-104, 2009).

CCN2 Gene and its Encoded Protein

Of all the six members of the CCN family, CCN2 has emerged as animportant player in its roles in the regulation of certain cellularfunctions important in skeletal growth, placental angiogenesis and woundhealing, as well as its roles in certain diseases including fibrosis(including renal and diabetes associated fibrosis), vascular sclerosis,atherosclerosis, bone disease, vascular resistance, tumorigenesis and/orcancer cell growth.

CCN2 has been now shown to be a causal factor in renal fibrosis, andappears to act in a similar fashion in other fibrotic diseases,including but not limited to, those occurring in the liver, lungs,heart, skin, vasculature and peritoneum (Dean R. G., Balding L., CandidoR., Burns W. C., Cao Z., Twigg S. M., Burrell L, M. Connective tissuegrowth factor and cardiac fibrosis after myocardial infarction. Journalof Histochemistry & Cytochemistry. 53(10):1245-56, 2005; Shi-wen X.,Pennington D., Holmes A., Leask A., Bradham D., Beauchamp J. R., FonsecaC., du Bois R. M., Martin G. R., Black C. M., Abraham D. J. Autocrineoverexpression of CTGF maintains fibrosis: RDA analysis of fibrosisgenes in systemic sclerosis. Experimental Cell Research. 259(1):213-24,2000; Ozaki S., Sato Y., Yasoshima M., Harada K., Nakanuma Y. Diffuseexpression of heparan sulfate proteoglycan and connective tissue growthfactor in fibrous septa with many mast cells relate to unresolvinghepatic fibrosis of congenital hepatic fibrosis. Liver International.25(4):817-28, 2005; Sakamoto N., Sugimura K., Kawashima H Tsuchida K.,Takemoto Y., Naganuma T., Tatsumi S., Nakatani T. Influence of glucoseand inflammatory cytokines on TGF-beta1 and CTGF mRNA expressions inhuman peritoneal mesothelial cells. International Journal of MolecularMedicine. 15(6):907-11, 2005; Zarrinkalam K. H., Stanley J. M., Gray J.,Oliver N., Faull R. J. Connective tissue growth factor and itsregulation in the peritoneal cavity of peritoneal dialysis patients.Kidney International. 64(1):331-8, 2003). When expressed in increasedamounts, this CCN2 upregulated, for example, by transforming growthfactor-β (TGF-β), high glucose concentrations, mechanical stress,advanced glycosylation end products (AGEs), induces (among other things)the over-accumulation of, and sometimes improperly organized,extracellular matrix (ECM) molecules (e.g., collagen forms, andthrombospondin (TSP)). This ECM when organized makes the spaceseparating cells, and includes membranes, connective tissue, and evenbone. This abmormal production/accumulation/organization of ECM resultsin scarring and fibrosis/sclerosis, and improper bone formationincluding osteoporosis.

Studies with the renal system have provided evidence of the role forCCN2 as an important pathogenic factor in fibrosis/sclerosis in a numberof models of chronic kidney disease (CKD). Early reports had suggested apossible interactive role in CCN2 with TGF-β in skin fibrosis andscleroderma (Bradham D M et al, Connective tissue growth factor: acysteine-rich mitogen secreted by human vascular endothelial cells isrelated to SCR-induced immediate early gene product CEF-10. Journal ofCell Biology, 114:1285-1294, 1991).

The formation of sclerosis or fibrosis in the kidney is a commonresponse to severe or chronic forms of injury. In chronic kidney disease(CKD), there appears to be three predominant causal factors: metabolic,genetic, and hemodynamic. All of these factors can interact,particularly in diabetic nephropathy (DN), to drive progression. CCN2now appears to be a central, downstream mediator of the effects of thesethree elements. For example, pathological shear or stretching forceresulting from intraglomerular hypertension appears to stimulate theproduction of cytokines including CCN2. This same force appears to beresponsible for increased vascular permeability leading to bothproteinuria and an increased production of vasoactive hormones such asangiotensin (AG) II and endothelin, which in turn also elevate CCN2 andfurther enhance the mechanical force. The abnormal accumulation ofadvanced glycosylation end products (AGEs) that occur with the alteredmetabolism of glucose in DN may also work to both directly to increaseextracellular matrix (ECM) cross-linking and accumulation, as well as toincrease CCN2. The genetic background of the individual can influencethe elements of hemodynamics and metabolism and in turn the resultingpathways as described. Additionally, there is a likely influence ofgenetics on protein kinase C (PKC) activity and production of vasoactivehormones. In all cases, the chronic upregulation of CCN2 activity islikely to result in altered ECM turnover and increasing ECMaccumulation, producing fibrosis or sclerosis (In: ContemporaryDiabetes: The Diabetic Kidney, CE Mogensen & P. Cortes (eds), HumanaAcademic Publishers, Totowa, N.J., June 2006, Riser, B L et al. CCN2(CTGF) in the pathogenesis of diabetic renal disease: A target fortherapeutic intervention). These findings support the postulate thatCCN2 is a central downstream element in the progression of fibrosis, andas such provides a reasonable and novel target for both diagnostics andtherapeutic purposes. Additional support for this in renal fibrosis hascome from data in humans showing that the level of renal CCN2, and/orthat passing into the urine, can be measured and used to predict theonset of renal disease and/or fibrosis as well as to stage progression.This has been supported by a number of reports showing that the level ofCCN2 present in the kidney glomerulus, or even passing into urinepredicts the future onset, and stages renal disease (including fibrosis)(Kidney International, 64:451-458, 2003. Riser, B L et al, CCN2 (CTGF):as a possible predictor of diabetic nephropathy: Preliminary report,Cytokine, 47, 1:37-42 2009, FK Tam, et al, Urinary monocytechemoattractant protein-1 (MCP-1) and connective tissue growth factor(CCN2) as prognostic markers for progression of diabetic nephropathy).

CCN2 is estrogen inducible and overexpressed in steroid-dependent breastor uterine tumors (Tsai et al., Expression and function of CYR61, anangiogenic factor, in breast cancer cell lines and tumor biopsies.Cancer Research 60: 5602-5607, 2000; Tsai et al., Expression andregulation of Cyr61 in human breast cancer cell lines. Oncogene 21:964-974, 2000; Sampath et al. Cyr61, a member of the CCN family, isrequired for MCF-7 cell proliferation: regulation by 17 beta-estradioland overexpression in human breast cancer. Endocrinology 142: 2540-2548,2001; Sampath et al., Aberrant expression of Cyr 61, a member of the CCNfamily (i.e. CCN1), and dysregulation by 17 beta-estradiol and basicfibroblast growth factor in human uterine leiomyomas. Journal ofClinical Endocrinology and Metabolism, 86: 1707-1715, 2001; Sampath etal, The angiogenic factor Cyr61 is induced by progestin R5020 and isnecessary for mammary adenocarcinorma cell growth. Endocrine, 18:147-150, 2002; Xie et al., Breast cancer, Cyr61 is overexpressed,estrogen-inducible, and associated with more advanced disease. Journalof Biological Chemistry, 276: 14187-14194, 2001; Xie et al., Elevatedlevels of connective tissue growth factor, WISP-1, and CYR61 in primarybreast cancers associated with more advanced features. Cancer Research,61: 8917-8923, 2002). CCN2 and other CCN family members are importantdownstream mediators of estrogen- and progesterone-regulated cellgrowth. CCN2 and other CCN proteins may also impact other growthregulatory pathways in breast cancer cells. Uterine CCN2 is regulated byboth estrogen and progesterone and appears to be important formaintenance or remodeling of stromal ECM (Rageh et al., Steroidalregulation of connective tissue growth factor (CCN2; CTGF) synthesis inthe mouse uterus. Molecular Pathology, 56: 80-85, 2001; Cheon et al., Agenomic approach to identify novel progesterone receptor regulatedpathways in the uterus during implantation. Molecular Endocrinology, 16:2853-2871, 2002). In the ovary, CCN2 is regulated by gonadotropins ortransforming growth factor-beta (TGF-β) and is associated with thecalcell recruitment and mitosis, and maintenance of the corpus luteum(Wandji et al., Messenger ribonucleic acids for MAC25 and connectivetissue growth factor (CTGF) are inversely regulated duringfolliculogenesis and early luteogenesis. Kidney International, 60:96-105, 2000; Slee et al., Differentiation-dependent expression ofconnective tissue growth factor and lysyl oxidase messenger ribonucleicacids in rat granulose cells. Endocrinology, 142: 1082-1089, 2001;Harlow & Hillar, Connective tissue growth factor in the ovarianparacrine system. Molecular and Cellular Endocrinology, 187: 23-27,2002; Harlow et al., FSH and TGF-beta superfamily members regulategranulose cell connective tissue growth factor gene expression in vitroand in vivo. Endocrinology, 143: 3316-3325, 2002; Liu et al.,Gonodotrophins inhibit the expression of insulin-like growth bindingprotein-related protein-2 mRNA in cultured human granulose-luteal cells.Molecular Human Reproduction, 8: 136-141; 2002).

U.S. Pat. No. 7,780,949 by Riser and DeNichilo discloses the role ofCCN2 in the production of extracellular matrix (ECM), as well as methodsfor diagnosing the presence and progress of pathologies characterized byan accumulation of the ECM components by measuring the level of CCN2 ina sample. The method is directed to diagnosing kidney fibrosis andassociated renal disorders, in particular, complications associated withdiabetes, hyperglycemia and hypertension.

CCN3 Gene and its Encoded Proteins

CCN3 is another member of the CCN family. It has been reported that CCN3exists in various forms. In a study to construct retroviral competentovian recombinants, it has been demonstrated that the CCN3 protein canbe expressed either as a full-length protein with a molecular weight ofabout 50 kDa or a smaller truncated protein, which is a fragment of thefull length protein (Perbal B., J. Clin. Pathol: Mol Pathol. 54: 57-79,2001). Other forms of CCN3 protein have also been reported. For example,a CCN3 related protein has been detected at the nuclear envelope of theNCI-H295R cells and another CCN3 related protein binds the promoter ofhuman plasminogen activator inhibitor type 2 (PAI-2) (Perbal B., J.Clin. Pathol: Mol Pathol, 54: 57-79, 2001). K19M-AF antibody directedagainst C-terminal 19-amino acid peptide of CCN3 revealed at least twoconformational states of the native CCN3 protein (Kyurkchiev S. et al.,Potential cellular conformations of the CCN3 (NOV) protein. CellularCommunication and Signaling, 2: 9-18, 2004). Cytoplasmic and cellmembrane bound CCN3 has an exposed C-terminus while secreted CCN3 has asequestered C-terminus which could be due to interaction with otherproteins or itself (dimerization).

The amino acid sequences of the full length CCN3 proteins from variousspecies, including human, have been fully characterized and aredisclosed by Li et al. (Li, C. L. et al., A role for CCN3 (NOV) incalcium signaling. Journal of Clinical Pathology: Molecular Pathology,55: 250-261, 2002). One CCN3 full length protein has about 357 aminoacids.

U.S. Pat. No. 7,780,949 by Riser discloses that the full-length CCN3molecule blocks fibrosis in an in vitro model of renal fibrosis byacting, at least partially, through its ability to down-regulate theprofibrotic activity of CCN2. CCN3 was not previously known to haveactivity in fibrosis or wound healing/scarring, either as a positive ornegative factor and was not known to have a regulatory effect on CCN2.U.S. Pat. No. 7,780,949 shows that the full-length CCN3 proteins canwork to inhibit the production and actions of CCN2, and thus theoverproduction of extracellular matrix that characterizes fibrosis inmany organs. Neither the above patent, nor other patents or publishedliterature, disclose whether a smaller portion of the whole CCN3, or apeptide, is capable of mediating this activity. It is now understoodthat fibrosis, although initiated by a variety of different insults,once started appears to follow a common pathway apparently alwaysinvolving one, or both of TGF-beta and CCN2 as causal factors.Therefore, having shown that CCN3 can be used to prevent and or treatfibrosis and abnormal production/accumulation of ECM e.g., collagen, inrenal cells and renal disease, one can reasonably assume that it will beuseful in such disease in other organs, and even those initiated bydifferent stimuli or insults. U.S. Pat. No. 7,780,949 further disclosesmeasuring CCN3 levels for diagnosis and prognosis of renal disease.

United States Patent Application Publication No. 2007/0059314 disclosesthe use of CCN3 or CCN3 fragments having angiogenesis-inhibitingactivity for the treatment of pathologies requiring such inhibitoryactivities. The fragments that exhibit angiogenic-inhibiting activityare approximately 40 to approximately 180 amino acids.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows in a very simplistic manner, the general multimodularstructure of the CCN proteins. CT, cysteine knot containing family ofgrowth regulators-like domain; IGFBP, insulin-like growth factor bindingprotein-like domain; TSP1, thrombospondin-like domain; and VWC, VonWillebrand factor-like domain.

FIG. 2 shows a published mouse sequence of CCN3 (SEQ. ID. No 41) usedfor design of peptides (upper sequence), and our modified sequence (SEQ.ID. No. 42) with the replacement of cysteines with serines, which doesnot exist in nature (lower sequence).

FIG. 3 shows specific sequences (peptides 1-40 disclosed as SEQ. ID.Nos. 1-40) that were tested for activity.

FIG. 4 shows the overall structure and sequence alignment of human CCN(hCCN), showing both hCCN2 (SEQ. ID. No. 43) and hCCN3 (SEQ. ID. No. 44)as the computer aligned them, with a schematic diagram of the fourdescribed modules shown in the upper part of the figure, includingIGF-BD, VWF, TSP and the c-terminal repeat element. The lower portion ofthe figure shows the sequence alignment (marked by asterisks) of the twomolecules (hCCN2 and hCCN3) here with the cysteines intact.

FIG. 5 shows the position of the synthesized CCN peptides (CCNp) onmouse CCN3 (SEQ. ID. No. 42) sequence showing the 35 constructedoverlapping sequences (CCNp1-35) beginning at the n-terminal end andrunning to the c-terminal end in black as well as the 5 specificallydesigned peptides CCNp 36-40 bolded (all here with the cysteinesreplaced with serines);

FIG. 6 shows the CCN3 sequences chosen for peptide design which weretargeted based on their position in the molecule and sequence homologywith CCN2. Ultimately, the cysteines were replaced with serine to avoidpotential formation of circular structures produced by the charge of thecysteine and thus the obliteration of the normal, or targeted functionwe were seeking. However, we also did not know if this change wouldresult in complete loss of the functions sought. These peptides were atthe same time chosen also for their high homology between human andmurine, so that any sequence tested in and proven effective in murinemodels would be expected to provide a same level of efficacy in humans.FIG. 6 discloses SEQ. ID. Nos. 45-49, respectively, in order ofappearance.

FIG. 7A shows the specific CCNp37 (SEQ. ID. No. 37) and CCNp38 (SEQ. ID.No. 38) peptides that were synthesized and tested having the cysteineresidues replaced by serine residues.

FIG. 7B is a comparison showing there is 100% homology between murineand human natural sequences of CCNp37 (SEQ. ID. Nos. 48 and 63,respectively, in order of appearance). Also, shown is there is one aminoacid difference between native human and mouse CCNp38 sequences,respectively (SEQ. ID. Nos. 50 and 49).

FIG. 7C shows a comparison of naturally occurring human CCN2 and CCN3sequences at regions selected for CCNp37 and CCNp38. For CCNp37 sequencechosen, both CCN2 and CCN3 have an unusual high homology over thesesequences at regions, with only one amino acid difference out offourteen. In great contrast, for the CCNp38 sequence chosen, CCN2 andCCN3 have an unusually low amino acid homology with only four alike outof fourteen amino acids. FIG. 7C discloses SEQ. ID. Nos. 51 (firstitem), 63 (second item), 64 (third item) and 50 (fourth item),respectively, in order of appearance.

FIG. 7D shows a comparison of naturally occurring murine CCN2 and CCN3sequences at regions CCNp37 and CCNp38. For CCNp37 there is nodifference from what was shown in 7C above, since there are nodifferences between human and mouse over this sequence. For CCNp38,there are 4 of 14 amino acids that match the sequence of CCN2 in thenaturally occurring sequences. FIG. 7D discloses SEQ. ID. Nos. 48, and49, second and fourth items respectively, in order of appearance. FIG.7D discloses SEQ ID NOS 65 and 66, first and third items, respectively,in order of appearance.

FIG. 7E shows peptide sequences with SEQ. ID. Nos. 37, 48 and 63, 54,and 55 in order of appearance.

FIG. 7F shows peptide sequences with SEQ. ID. Nos., from top to bottomof 38, 49, 56, 50, 53, 52, 59, 60, 57, 58, and 61.

FIG. 8 shows that CCNp37 and CCNp38 reduce collagen promoter stimulationby TGF-β. Peptide 38 (TOP) was able to inhibit collagen promoteractivity at 500 ng/mL. Peptide 37 demonstrated an ability to totallyblock TGF-β-stimulated collagen promoter activity when added just priorto TGF-β (right 3 bars in lower figure). This inhibitory activity wasalso present (although to a lower level) even when added 24-hours priorto TGF-β. None of the other 38 peptides made and tested showed activityin this assay, so the data are not shown. The Y-axis in the top figureis the level of collagen promoter activation (in arbitrary units), basedon a transfection efficiency control (CMV promoter activation), as alsoshown in the lower figure.

FIG. 9 shows CCNp37 and CCNp38 dose-dependently blocking the cellularadhesion to CCN2 coated plates. Control plates show the adhesion ofrodent mesangial cells to plastic only (uncoated) plates. “CTGF” orCCN2, the second bar from the left, shows the marked increased adhesionmediated by cellular receptor binding to CCN2-coated plates, as opposedto that occurring on the uncoated plastic. Full-length CCN3 (NOV) human(27 nM) added just prior to the treatment with TGF-β, provided someinhibition of this binding as expected. However, peptides CCNp37 andCCNp38 dose-dependently blocked the receptor binding mediated to CCN2,providing approximately 60% to 70% inhibition at the highestconcentration tested (500 nM). This indicates that the two peptides areeach able to interact at the binding site. None of the other 38 peptidestested (only p35, p36, p37 and p40 of those shown here for spaceconsiderations) were able to as strongly block binding. The specificactivity shown for peptides CCNp37 and CCNp38 in this assay demonstratean ability to block the receptors on the cells that would bind CCN2, andwould be required for specific activities. Cellular adhesion and thebinding of the peptide to the receptor for CCN2 is critical to normalphysiology and numerous pathological states.

FIG. 10A shows CCN2 immunolocalization (reactivity with protein specificantibody) and the inhibitory effect of peptide CCNp37. Here shown, TGF-βtreatment results in a dramatic loss (secretion) of the already madeCCN2 localized at the cell membrane (dark reddish brown) but alsoinitiates the synthesis of new CCN2, now seen in the cytoplasm (lightreddish brown). Along with this, is a phenotype change to a moreelongated angular, fibroblast-type cell, characteristic of that seen infibrosis. Treatment with CCNp37 at 50 nM blocks this phenotypictransition, and reduces greatly the expulsion of CCN2 and synthesis ofnew CCN2.

FIG. 10B shows CCN2 immunolocalization and the inhibitory effect ofpeptide CCNp38. The untreated control cells show extensive CCN2 (brown)at the cell borders. TGF-β treatment results in a dramatic loss(secretion) of CCN2 at the cell membrane and the initiation of newsynthesis now seen throughout the cytoplasm. Along with this is aphenotype change to what appears to be a fibroblast-type cells,characteristic of fibrosis. Treatment with CCNp38 blocks this phenotypictransition, the expulsion of CCN2, and new synthesis of CCN2. Theoptimal effect appears to be at 50 nM, with a dose response effectoccurring with lower concentration. Other peptides did not produce thiseffect (not-shown).

FIG. 11A shows collagen I immunolocalization and the inhibitory effectof peptide CCNp37. TGF-β (a potent stimulator of collagen accumulationand fibrosis) treatment results in a dramatic loss or secretion of theabundant collagen I at the cell membrane (shown in the control frame asbrown or reddish brown) and the initiation of some new synthesis seenthroughout the cytoplasm (TGF-β treated). Along with this is a phenotypechange to what appears to be an elongate, less cuboidal, fibroblast-typecell characteristic of fibrosis. Treatment with CCNp37 at a lowconcentration of 0.5 nM blocks this phenotypic transition, the expulsionof CCN2 and new synthesis of CCN2. Higher doses show the same or similareffect. Other CCNp peptides tested did not show this effect (not shown).

FIG. 11B shows collagen I immunolocalization and the inhibitory effectof peptide CCNp38. Treatment with TGF-β (a known pro-fibrotic agent)results in a dramatic loss (secretion) of the abundant collagen I at thecell membrane (shown in the control frame) and the initiation of somenew synthesis seen throughout the cytoplasm (TGF-β treated). Along withthis is a phenotype change to what appears to be an elongate, lesscuboidal, fibroblast-type cell. Treatment with CCNp38 at lowconcentration of 0.5 nM has little effect. However, at doses of 5-50 nMthere is a blockade of the phenotypic transition, the expulsion of someof the premade collagen and new synthesis of collagen that occurs inresponse to TGF-β. Other peptides did not demonstrate this effect (notshown).

FIG. 12A shows a bar graph of cell proliferation of human chronicmyelogenous leukemia in untreated cells (Control) and compared to thosepre-incubated with quantities (about 10 nM) of a commercial recombinantCCN3 (rCCN3c) (SEQ. ID. No. 67), full length CCN3 protein made in ourlaboratory rCCN3 8 (SEQ ID NO: 44), rCCN3 9 (SEQ ID NO: 44), rCCN3 10(SEQ ID NO: 44), rCCN3 11 (SEQ ID NO: 44), or CCNp37 or CCNp38. CIVILcells were allowed to grow, then proliferation measured by theCellTiter-Glo®Luminescent Cell Viability Assay Control untreated cells,or cells. The latter is a homogeneous method of determining the numberof viable cells in culture based on quantitation of the ATP present, anindicator of metabolically active cells. The commercially produced fulllength CCN3 produces an approximate 35% reduction in growth and/orviability over the period tested. CCNp37 produces 15-20% inhibition andCCNp38 approximately 40% inhibition, i.e., greater than the effect offull length CCN3.

FIG. 12B shows the tests of CCNp37-1 (SEQ. ID. 37) and CCNp38-1 (SEQ.ID. 38) for their ability to inhibit the growth of chronic myelogenousleukemia cells (CIVIL) in culture and a comparison to rCCN3 (SEQ. ID.NO: 67). Both peptides were able to strongly slow the growth of chronicmyelogenous leukemia cell growth.

FIG. 13 demonstrates the increased human skin fibroblast proliferationin response to gadolinium (GAD) a contrast agent used in MM diagnostics,and thought to cause a pathology termed nephrogenic systemic fibrosis(NSF), when not cleared by the kidneys and deposited in the skin.

FIG. 14 shows that human skin fibroblasts produce and secrete CCN3 inculture under basal conditions, and the exposure to GAD dose-dependentlydecreases this CCN3 production, while at the same time increasing cellproliferation (compare to FIG. 13). This suggested that CCN3 is able tocontrol fibroblast proliferation. This is important since, NSF, andcertain other fibrotic diseases are characterized as fibroproliferativediseases. In these instances proliferation of a key effecter cellresults in the overaccumulation of ECM, i.e., collagen, and fibrosis.Previous studies have shown the cytokine platelet derived growth factor(PDGF) production by skin fibroblasts drives the response to GAD. Theerror bars in the figures represent standard error.

FIG. 15 demonstrates that human fibroblast proliferation is increased byPDGF and this stimulation is blocked by the addition of CCN3 protein aswell as CCNp38-3 (Seq. ID. No. 56).

FIG. 16 shows that TGF-beta does not stimulate cell proliferation inthis model, and neither CCN3 (SEQ. ID. No. 67) nor CCNp38-3 (Seq. ID.No. 56) has an effect on baseline cell growth, indicating specificity ofresponse. Extracellular matrix (ECM) accumulation is a dynamic processmade up of both regulated synthesis and breakdown (ECM turnover).Accumulation or overaccumulation in fibrosis is the result of animbalance in the two and can therefore be the result of increasedsynthesis or decreased synthesis rates. However, fibrosis is oftencharacterized by an increase in both synthesis and breakdown, i.e.,increased turnover and results from the net difference. Amongactivities, matrix metalloproteinase 1 (MMP-1) acts to increasebreakdown, whereas tissue inhibitors of MMP (e.g., TIMPs) reduce theactivity of MMP.

FIG. 17 shows that PDGF exposure also acts to increase MMP-1 activity,whereas CCN3 is able to block that increase. CCNp38-3 (Seq. ID. No. 56)works as well or better than CCN3 protein to accomplish this blockade.

FIG. 18 shows no stimulating effect of TGF-beta and therefore no effectof CCN3 or the peptide.

FIG. 19 shows that PDGF also acts to increase TIMP-1 production andneither CCNp38-3 (Seq. ID. No. 56) nor CCN3 (SEQ. ID. No. 67) is able toblock or reduce the increase in TIMP-1 production, showing specificityof response.

FIG. 20 shows that TGF-beta fails to stimulate TIMP-1 production andneither CCNp38-3 or CCN3 have an effect.

FIG. 21 shows that TGF-beta exposure increases pro-collagen production2-fold or greater and both CCN3 ((SEQ. ID. No. 67) and CCNp38-3 (Seq.ID. No. 56)) completely block the increase.

FIG. 22 shows, human skin fibroblast proliferation in response to PDGFand the effect of 1 nM CCN3 or CCNp peptide as expected, PDGF exposureproduced a strong increase in cell proliferation. rCCN3 (SEQ. ID. No.67) alone slightly decreased proliferation whereas all of the peptideshad a similar or greater reduction (8-22%) in proliferation.

FIG. 23 shows human skin fibroblast proliferation in response to PDGFand the effect of 10 nM CCN3 or CCNp peptide. CCN3 alone produced a 33%reduction in proliferation, whereas the CCNp peptides produced a similar19-30% inhibition.

FIG. 24 shows human skin fibroblast proliferation in response to PDGFand the effect of 100 nM CCN3 or CCNp peptides. CCN3 alone produced a46% reduction in proliferation, whereas the CCNp peptides produced asimilar 19-36% inhibition. Taken as a whole there was a dose-dependentefficacy of CCN3 and all of the peptides in this group, although therewere some differences in the CCNp peptides dependent on themodification.

FIGS. 25-27 show the test results of the effect of modifications inCCNp37 and CCNp38 on their ability to block PDGF stimulated MMP-1production, as a measure of their effectiveness in blocking skinfibrosis/scarring.

In FIG. 25 CCN3 at 1 nM was able to block little or no MMP-1 production,whereas all of the peptides tested in this series blocked significantlyat 1 nM (16-44%). In FIG. 26, the effect of CCN3 at 10 nM was increased(to 27% reduction in MMP-1), whereas the CCNp peptides in some casesincreased their activity to as much as 60% inhibition. In FIG. 27 at 100nM CCN3 reached a 30% reduction in the stimulated MMP-1 production,whereas all CCNp peptides had similar or stronger activity, withCCNp38-3 and CCNp38-4 blocking up to about 60%. All peptide variantswere able to block a marked level of MMP-1 production, including thosewith either cysteine intact or a replacement with serine. When CCNp37and CCNp38 was made slightly shorter or longer this produced a smallchange in the effectiveness of the molecule. Some, particularly,CCNp37-15 (SEQ. ID. No. 55) that was slightly reduced in size on thec-terminal end was less effective however.

FIGS. 28-30, show the test results of the same series of peptides fortheir ability to block PDGF stimulated TIMP-1 production, as a measureof their effectiveness to alter the accumulation of ECM and thus skinfibrosis/scarring. TIMP-1 production is known to be associated with areduction in ECM breakdown and thus reduced turnover. CCN3 was unable toblock the increase in TIMP-1 stimulated by PDGF (FIGS. 29 and 30, CCN3not tested in FIG. 28). Most of the peptides were also unable to alterthe production of TIMP-1. However, CCNp37-12 (Seq. ID. No. 37) andCCNp38-1 (Seq. ID. No. 38) unexpectedly produced approximately 50 and70% reduction respectively (FIG. 30). CCNp38-3 (Seq. ID. No. 56), 38-4(Seq. ID. No. 50), and 38-9 (Seq. ID. No. 57) were tested at the highdose only.

FIGS. 31-33 show the test results of the effect of modifications inCCNp37 and CCNp38 on TGF-beta-stimulated human fibroblast pro-collagenproduction and compared the effect to that of CCN3 (Seq. ID. No. 67), todetermine their suitability as therapeutic agents. As expected TGF-betasignificantly increased the production of pro-collagen type 1 whereasCCN3 was able to block up from 66 to approximately 86 percent of thestimulated pro-collagen production as the dose was increased (1-100 nM).All of the peptides tested except CCNp 37-12 (Seq. ID. No. 37) were ableto reduce the stimulation of pro-collagen type 1 production to somedegree. CCNp38-3 (Seq. ID. No. 56) however, was as effective as CCN3(Seq. ID No. 67].

FIG. 34 shows the method or protocol used to test efficacy of peptideCCNp38 in an animal model of diabetic renal disease. This was carriedout using the BT/BR Ob/Ob mouse strain that has a defective leptinreceptor that results in increased appetite. As a result mice rapidlygain weight over the control strain and become hyperglycemia at aboutone month of age going on to develop renal disease resembling that inhumans. This is regarded by some to be the best rodent model formirroring renal disease in humans as a complication of diabetes. Animalswere treated with either rCCN3 (SEQ. ID. NO: 67) or CCNp38 (SEQ. ID. 38)beginning at 9 weeks of age, when early renal disease has beendocumented. Mice were treated for 8 weeks, then sacrificed and measuredfor renal disease and other complications, and the effect drugtreatment. Shown below the time line in the figure are the reportedrenal disease characteristics, and thus the expected manifestations ofdisease. Shown above the time line is the comparable progression inhumans.

FIG. 35 shows that 17 weeks of diabetes elevates plasma creatinine,substantiating impaired renal function, and 8 weeks of treatment withCCN3 (SEQ. ID. NO: 67) or CCNp38 (SEQ. ID. 38), reduces or blocks thisimpairment.

FIG. 36 shows that 17 weeks of diabetes elevates the albumin tocreatinine ratio, substantiating protein leakage and renal damage, and 8weeks of treatment with CCN3 or CCNp38 greatly blocks this renal damageas evidenced by the lack of change.

FIG. 37A shows qualitatively by PAS staining, in gray scale that 17weeks of diabetes results in mesangial expansion, substantiating renalfibrosis (white stain shows collagen deposition). FIG. 37B showsquantitatively by image analysis of multiple PAS stains (3 sections permouse/7-9 mice per treatment group) that 17 weeks of diabetes results inmesangial expansion, substantiating renal fibrosis., and 8 weeks oftreatment with CCN3 or CCNp38 greatly blocks this pathology.

FIG. 38 shows that renal mRNA levels for the fibrosis gene CCN2 areincreased by diabetes, and treatment with CCN3 or CCNp38 greatly reducesor blocks the increase, thus treating the disease.

FIG. 39 shows that renal mRNA levels for the fibrosis gene Col1A2 areincreased by diabetes, and treatment with CCN3 or CCNp38 greatly reducesor blocks the increase, thus treating the disease.

FIG. 40 shows that renal mRNA levels for the control 18S rRNA are notincreased by diabetes as expected, and treatment with CCN3 or CCNp38 hasno effect on levels as expected.

FIG. 41 shows that liver weight is greatly increased by 18 weeks ofdiabetes, and treatment with CCN3 or CCNp38 slightly reduces thisincrease.

FIG. 42 shows that liver mRNA levels for the fibrosis gene CCN2 areincreased by diabetes, substantiating an inflammatory response andinitiation of fibrosis, treatment with CCN3, but particularly CCNp38greatly reduces or blocks the increase in a dose-dependent manner.

FIG. 43 shows that liver mRNA levels for the fibrosis gene Col1A2 areincreased by diabetes, substantiating the initiation of fibrosis,treatment with CCN3 reduced, but again CCNp38 dose-dependently blockedthe increase in collagen.

FIG. 44 shows that heart mRNA levels for the fibrosis gene plasminogenactivator inhibitor 1 (PAI-1) are increased by diabetes, substantiatingthe initiation of fibrosis, treatment with CCNp38 greatly reduces, andat the high dose blocks the increase,

DETAILED DESCRIPTION OF THE INVENTION

While this invention is susceptible of embodiments in many differentforms, there is shown in the figures, and will be described herein indetail, specific embodiments thereof with the understanding that thepresent disclosure is to be considered as an exemplification of theprinciples of the invention and is not intended to limit the inventionto the specific embodiments illustrated.

The present invention is directed to isolating newly described, newlyproduced, specific, effective CCN derived peptides, as a substitute forthe full-length CCN3 protein, to achieve equal or better anti-CCN2 andanti-fibrotic activity, also producing novel manufacturing and deliveryadvantages. In a preferred form of the invention, it was surprisinglyfound that a small number of peptides having from about 12 to about 20,more preferably 12 to about 18 and most preferably 12 to about 15 aminoacids and most preferably fourteen amino acids in human, mouse and ratnative sequences and in analogs of the same where native cysteineresidues are substituted with a replacement amino acid are able to mimicspecific activities of CCN3. In a preferred form of the invention, thereplacement amino acids are selected from serine, alanine, glycine,S-methylated cysteine or a combination thereof. Most preferably, thereplacement amino acid is serine. These peptides were effective intreating pathologies associated with the over-accumulation,disregulation of turnover, or altered composition, of extra-cellularmatrix proteins. These short peptides are far smaller than thefull-length CCN3 protein, the naturally occurring one-half andone-quarter length CCN3 fragments reported in the literature, and theartificially prepared 40 to 180 amino acid fragments disclosed in the'314 published patent application discussed above, and are likely to bemore easily synthesized and formulated for delivery to a patient in needthereof. Sometimes these small peptides may be referred to as “CN”followed by a number, e.g., CN38 as a shorthand for CCNp38.

Selection of the CCN3 Peptides

The present invention discloses a role of CCN3, or CCN2, derivedpeptides in among others, diseases associated with theover-accumulation, disregulation of turnover, or altered composition ofextracellular matrix molecules in a human subject, which can lead tofibrosis, scarring, abnormal wound healing and cancer cell/tumor growthand metastasis. Certain CCNp peptides of the present invention can beused, in some cases, as a substitute for full-length CCN3 protein, toachieve equal or greater anti-fibrotic activity. The term “fibrosis”used in the present disclosure is used interchangeably with the term“sclerosis” and “scar formation” since they are similar processesinvolved in the overgrowth of fibrous or fibrosis-like tissue and/or theincreased, abnormal deposition and/or assembly/organization ofextracellular matrix molecules such as collagen, and all may have CCN2as at least a causal factor.

In order to isolate the CCN peptides, a series of 36 short overlappingpeptide sequences, beginning at, and defined by, the n-terminal regionand working to the c-terminal end of the CCN3 were generated. Shortoverlapping sequences are defined herein as sequences ranging in sizefrom about 12 to 20 amino acids and more preferably 12 to 18 amino acidseven more preferably 12-15 amino acids and most preferably 14 aminoacids (or any range or combination of ranges therein) and overlap eachother on the full-length protein sequence by about 3 to 7 amino acids.Murine (rodent) models of fibrosis were first used to verify fibroticactivity; therefore murine CCN3 sequences were used. It is well-known inthe art that human CCN3 has a strong homology with rodent. In fact, themouse and the human sequences for the region chosen for peptide CCNp37are identical, whereas for CCNp38 there is only a single amino aciddifference between the human and the mouse. FIG. 2 shows the publishedmouse CCN3 sequence and the location of cysteine residues that werereplaced here by serine residues, in order potentially to aid in theprevention of circularization of the peptides, and loss of activity. Onthe negative side, this substitution could also have the potential toeliminate all biological activity ascribed to CCN3, especially since itis known to be a “cysteine-rich molecule” and its known function wouldtherefore be expected to be dependent on the presence of cysteines. Theeffect(s) of this change could not be predicted before our work. Thecysteine-modified peptide sequences shall sometimes be referred to asanalogs or serine analogs of CCN3 native sequences. FIG. 3 shows thesequence of the overlapping peptides that were synthesized and tested(peptides designated CCNp1-35).

The following table coordinates the peptide numbers with the SEQ. ID.Nos. and a representative figure where the sequence is shown.

SEQ. ID. REPRESENTATIVE NO. DESCRIPTION FIGURE 1-40 CCNp1 through CCNp40See FIG. 3 41 Mouse native CCN3 full-length See FIG. 2 42 Mouse analogCCN3 full-length with native See FIG. 5 cysteines replaced with serines44 Human native full-length CCN3 See FIG. 4 45 Mouse native CCNp39206-220 See FIG. 6 first item 46 Mouse native of CCNp40 213-227 See FIG.6 second item 47 Mouse native CCNp36 See FIG. 6 third item 63 and Humanand mouse native CCNp37 289-302 See FIG. 6 fourth item and 48, FIG. 7Csecond item respectively 49 Mouse native CCNp38 84-98 See FIG. 6 lastitem 50 Human native CCNp38 See FIGS. 7B and 7C 51 CCN2 native fragmentwith high homology with See FIG. 7C native CCN3 52 Rat native CCNp38 SeeFIG. 7F 53 Rat analog CCNp38 with native cysteines replaced See FIG. 7Fwith serines 54 Human or mouse analog CCNp37-14 with native See FIG. 7Ecysteines replaced with serines and without FS on N-terminal end 55Human or mouse analog CCNp37-15 with native See FIG. 7E cysteinesreplaced with serines and without PH on C-terminal end 56 Human analogCCNp38-3 with native cysteines See FIG. 7F replaced with serines 57Human analog CCNp38-9 with native cysteines See FIG. 7F replaced withserines and minus CD (or SD) at N- terminal end 58 Human analogCCNp38-10 with native cysteines See FIG. 7F replaced with serines andwith added T on C- terminal end 59 Mouse analog CCNp38-7 with nativecysteines See FIG. 7F replaced with serines and without CD or (SD) at N-terminal end 60 Rat analog CCNp38-8 with native cysteines See FIG. 7Freplaced with serines and without CD or (SD) at N- terminal end 61 Humannative CCNp38-11 with a T added to the C- See FIG. 7F terminal end 62Human analog full-length CCN3 with native None cysteines replaced withserines

Since CCN2 and CCN3 are members of the same family, but possessdifferent apparent biological functions (in the case of effect oncollagen it was found opposite activities), this suggested to us that atleast one mechanism for the observed blocking activity of CCN2 (anddownstream collagen production) might be due to receptor competition.That is, CCN3, or a part of it, might interact with a CCN2 receptorpreventing or interfering with CCN2-mediated signaling. That is, CCN3might possess a sequence that is recognized by the CCN2 receptor, butwhen bound to it, would not allow signaling for increase matrixproduction or accumulation, i.e., it could act as a natural, competitor.This was not an obvious mechanism, however, because we also found thatCCN3 also greatly inhibited CCN2 synthesis, so it remained possible thatthe activity was not due to a receptor blockade, but instead due to aninhibition in the production of CCN2. Nevertheless, the two proteins,CCN3 and CCN2, were examined for similarities and differences in aminoacid sequence (structure), after producing a computer-generated“best-fit” alignment as shown in FIG. 4 starting with the humansequence. For the reasons hypothesized above, four regions with veryhigh complementary in amino acid sequences (i.e., between CCN2 and CCN3)were found and chosen from both the TSP-like element (referred to asCCNp39, CCNp40, and CCNp36) and the C-terminal module (referred to asCCNp37) (FIGS. 4 and 5). Also selected was one region within theinsulin-like growth-factor binding domain of CCN3, referred to asCCNp38, where it was observed that CCN3 and CCN2 had unusually low (14%in murine, 28% in human) complementary over a relatively large region(shown in FIGS. 4 and 5). It was possible that this unique differencediscovered might be responsible for the different actions of CCN2 versusCCN3, and might work to block CCN2, work independently, or in additionto CCN2 blockade. All of the peptide sequences, namely CCNp39, CCNp40,CCNp36, CCNp 37 and CCNp38, were further reduced by replacing anycysteine residues with serine residues. Consequently, such serinemodified peptide sequences are derived from CCN3 sequences and couldpossibility possess similar anti-fibrotic activity as we observed withthe full-length protein. It is also contemplated that the cysteineresidues could also be replaced by alanine, glycine, S-methylatedcysteine or combinations thereof (including serine) to produce similaractivity.

The present invention contemplates that the CCN3 peptide sequences andtheir analogs discovered have the same, similar, or greater CCN2inhibitory, and ECM (e.g., collagen) regulating activity as the fulllength protein. As discussed in further detail below, we were surprisedto find that two short peptides, CCNp37 and CCNp38, demonstratedsignificant CCN2 inhibitory activity while the 38 other peptidesscreened were not effective in inhibiting CCN2 expression. Thus, thesepeptides are unique and useful in the treatment of pathologiesassociated with the over-accumulation, disregulation of turnover, oraltered composition of extracellular matrix molecules in the subject.

FIG. 6 shows the sequences chosen for the 4 specifically designed andmade peptides (36-40) and states the approximate homology to the bestmatching of the CCN2 sequence. Three were chosen for their high homology(CCNp37, 39, 40) to CCN2 sequences, one for its low homology (CCNp38),and one for its average (50%) homology (p36). More particularly, FIG. 7Ashows peptide sequences CCNp37 and CCNp38 that were selected andsynthesized by replacing the cysteine residues with serine to possiblyprevent circularization of the molecule and loss of activity. Asdiscussed above, murine peptides were selected for testing because ofits high degree of homology with humans which is illustrated in FIG. 7B,and the use of murine models to demonstrate efficacy, predicting thehuman response. The human equivalent sequence to the tested murineCCNp38 is shown in FIG. 7B bottom. There is only one amino aciddifference between this sequence in humans and mice (bottom sequenceFIG. 7B and bottom sequence FIG. 7D). Finally, FIG. 7C and FIG. 7Ddemonstrate that while a strong homology exists between CCN2 and CCN3 atthe peptide sequence of CCNp37, that same homology does not exist atpeptide sequence CCNp38.

Results from the Screening of Selected CCN3 Peptides

The peptides selected above, and shown in FIG. 5, were synthesized andtested in the three different in vitro assays constructed to modelfibrosis, or fibrosis-related pathology in vivo for anti-fibroticactivity. These assays have been used extensively by us and by others,and are highly predictive of related responses in vivo, including thoseoccurring in humans. One in vitro assay, i.e., of cell adhesion in vitrowas used. There is a requirement for adhesion in wound healing andfibrosis, with cells responding to the binding of CCN2 to theirreceptors for other critical activities. Also alteration of cellattachment and receptor binding is implicated in other non-fibroticdiseases, previously named in this application. For this adhesion assay,a well of a culture plate was coated with CCN2 protein and then ratmesangial cells were added for a defined period. Since the mesangialcells possess CCN2 receptors, they bind tightly to the plate via thespecific receptor and therefore adhesion via this receptor can bemeasured. After a standard period of incubation, the cells are washed toremove non-attached cells. These adherent cells are then removed andcounted to determine the percent of the total cells that adhered. Theability of each peptide to block this binding was examined bypreincubating cells with the peptide of interest. Controls were used forcomparison without CCN2 coating.

In a second assay, the ability of the peptide to block the stimulationof collagen type I promoter by TGF-beta was tested. Collagen type Iupregulation is a characteristic feature of fibrosis and is often usedas an end point determination. TGF-beta is a well-establishedpro-fibrotic factor or cytokine that mesangial cells and other cells inthe fibrotic response respond to by upregulating collagen and othermatrix molecule production and accumulation. Several new anti-fibrotictherapies are under development that target the activity of TGF-beta.For the assays used in connection with the present invention, collagenpromoter activity was measured as a rapid and early indicator ofcollagen-related fibrotic activity. The cells in culture were eitherunstimulated or stimulated by TGF-beta, both in the presence and absenceof the selected peptides. If the peptides have inhibitory activity, thepromoter activity under TGF-beta stimulation would be reduced to somevalue approaching the control, non-TGF-beta treated cells. The collagenpromoter assay is based on the transfection of mesangial cells with aCOL 1a2 promoter linked to luciferase. Therefore, when the promoter isstimulated it can be measured as luciferase units (Riser et al, CCN3 isa negative regulator of CCN2 and a novel endogenous inhibitor of thefibrotic pathway in an in vitro model of renal disease, American JPathology, 174, 5, 2009). The level of collagen promoter activation (inarbitrary units), is based on a transfection efficiency control (CMVpromoter activation).

In a third assay, and immunochemical staining was developed that allowedfor measuring cellular changes in response to TGF-beta stimulation inboth the amount and distribution of CCN2 as well as collagen type I (aprototypical ECM molecule altered in fibrosis, atherosclerosis, vascularcalcification, bone disease, and other related disease). This assay alsoallows one to determine if there is a phenotype change of the cells,particularly to a more fibroblastic-like cell. This change ischaracteristic in fibrosis; not only in mesangial cell in renal fibrosisbut also other cell types can cause fibrosis. This assay is thereforeapplicable to test the effect of synthesized peptides (Riser et al, CCN3is a negative regulator of CCN2 and a novel endogenous inhibitor of thefibrotic pathway in an in vitro model of renal disease, American JPathology, 174, 5, and 2009).

The results from the peptide screens showed no significant inhibition ofCCN2-mediated binding or of collagen promoter-inhibitory activity forany of the 36 overlapping peptides in either the collagen promoter orthe CCN2-mediated adhesion assay. For peptide 37 (CCNp37) designed to aspecific region in the c-terminal module with high (nearly 100%)complementary, both inhibition of TGF-beta stimulated collagen promoteractivity (FIG. 8) was found, as well as inhibition of receptor binding(adhesion to CCN2) (FIG. 9). CCNp37 appeared to be more potent thanCCNp38 in inhibiting collagen promoter activity, and treatmentimmediately prior to TGF-beta was most effective (bottom figure right),however, even a 24 hour prior exposure was able to produce some activity(bottom center). CCNp37 and p38 also had marked, and similareffectiveness in inhibiting TGF-beta stimulated adhesion to CCN2. Thisdemonstrates a dose-dependent ability of CCNp37 and CCNp38 to interferewith CCN2 binding to its cellular receptor. None of the overlappingpeptides or those other specifically designed peptides showed anyconsistent inhibitory activity. Some peptides were even observed toenhance the promoter activity. CCNp38 has remarkably low complementaryto CCN2 and is found in the IGFBD domain. This positive effect of CCNp37and CCNp38 was also found when examined during immunohistochemicalstaining assay. CCNp37 (FIG. 10A) and CCNp38 (FIG. 10B) were able toblock the redistribution and new synthesis of CCN2 in a dose-dependentmanner indicating an effect on both production and activity of CCN2, andappeared to also block the transition to a fibroblast-type cell, andimportant factor in the transition of cells to a phenotype important inthe generation and progression of fibrosis in many organ systems. Asimilar blockade effect on collagen type I was observed and occurredwith both CCNp37 (FIG. 11A) and CCNp38 (FIG. 11B). The present inventiontherefore demonstrates for the first time, a method to block CCN2synthesis and activity, cell binding or adhesion to CCN2, collagenaccumulation, mesangial cell transition to a fibroblast-type cell andthus fibrosis, using unique small peptides from very limited selectiveregions of the full-length CCN3 protein. Consequently, the CCN3 peptideof the present invention may be also be used to block CCN2 mediatedstimulation of cancer cell growth and to promote wound healing withminimal scarring. Since CCN2 is well-known as a key factor in theprogression of a number of diseases, the ability to block this factor bysuch peptides has far reaching therapeutic applications. It wasunexpected finding that one region with near total complementary and onedifferent region with little or no complementary were both effective atblocking adhesion, CCN2 activity, adhesion and collagen activity. Thesefindings and activities could not be predicted.

One of the potential uses of the method in the present invention is forthe treatment of fibrosis. The term “fibrosis” used in the presentdisclosure includes fibrosis and/or sclerosis and scarring since theyare similar processes and virtually all have been shown to have CCN2 asat least one causal factor. In the present disclosure, “fibrosis”,“sclerosis” and “scarring” can be used interchangeably. The fibrosis canbe associated with any organ capable of forming fibrosis, such as (butare not limited to) kidney, heart, liver, lungs, vasculature (includingscleroderma, coronary arteries), skin, cervix, edometrium, eye, gums,brain, and the peritoneum. The fibrosis can also be the result of one ofthe pathological conditions such as (but are not limited to) renaldiseases, peritoneal dialysis, macular degeneration, periodontaldisease, congestive heart failure, cardiac ischemia and cardiachypertrophy, stroke and related ischemia and reperfusion injury,surgical and medical intervention procedures (e.g., balloon angioplasty,insertion of stents, catheters, grafts (including arterial and venousfistulas) and organ transplants) and unwanted post-surgical tissue ororgan adhesions and scarring. The fibrosis can also be associated withincreased cellular proliferation, for example, glomerular proliferativedisease and vascular stiffness caused by cell proliferation, medial andintimal calcification. Other indications are associated with abnormalcellular proliferation, for example, cancer, particularly when growth ormetastasis is related to upregulation of CCN2 expression,atherosclerosis, bone disease, osteophorosis, renal osteodystrophy,osteochondrodysplasia, osteitis fibrosa, osteoclastogenesis disease,vascular resistance, vascular calcification, tumorigenesis, andextracellular matrix disregulation. The pathology can be secondary to,the increased production/secretion and/or activity of TGF-β, woundhealing, chronic kidney disease, intraglomerular hypertension, cancercell growth, diabetes, inflammation, hyperglycemia, hypertension, renalproliferative disease, altered integrin receptor expression,extracellular matrix disregulation disease or connective tissue disease.

Results from a study of the effect of CCN3 peptides on the growth ofhuman chronic myelogenous leukemia cells.

Another potential use of the methods described in the invention is forthe treatment of cancers. CCN3 has been shown to play a role in limitingthe growth of certain cancers. CCNp generated to mimic the effects ofthe function of CCN3 to prevent, reduce, stop or reverse progression offibrosis/scarring may also serve to limit cancer growth. FIG. 12A showsa bar graph of cellular proliferation of human chronic myelogenousleukemia cells (K562) as percent of the growth of the untreated control.In untreated cells (Control) and those pre-incubated with quantities(approximately 10 nM) of a commercial recombinant CCN3 (rCCN3c), or fulllength CCN3 made in our laboratory, represented by several preparationsrCCN3 8 (SEQ ID NO: 44), rCCN3 9 (SEQ ID NO: 44), rCCN3 10 (SEQ ID NO:44), rCCN3 11 (SEQ ID NO: 44), or the peptides CCN p37 or CCN p38 wereallowed to grow, then proliferation measured by theCellTiter-Glo®Luminescent Cell Viability Assay Control untreated cells,or cells (McCallum, L et al, CCN3: a key growth regulator in ChronicMyeloid Leukaemia, J Cell Commun Signal. 2009 June; 3(2): 115-124). Thelatter is a homogeneous method of determining the number of viable cellsin culture based on quantitation of the ATP present, an indicator ofmetabolically active cells. Our results showed that the commerciallyproduced full length CCN3 (SEQ. ID. NO: 67) produces an approximate 35%reduction in growth and/or viability over the period tested. Incomparison, CCNp37 produces 15-20% inhibition and CCNp38 approximately40% inhibition of cell growth. Thus the activity was greater than thefull-length CCN3.

FIG. 12B shows the testing of CCNp37-1 (SEQ. ID. 37) and CCNp38-1 (SEQ.ID. 38) for their ability to inhibit the growth of chronic myelogenousleukemia cells (CIVIL) in culture and a comparison to rCCN3 (SEQ. ID.44). Both peptides were able to inhibit the growth of CML cells byslowing their replication time, and CCNp38-1 worked better than CCN3.Therefore, these CCNp peptides would be expected to be therapeutic inthe treatment of CIVIL, and other forms of cancer to reduce cell growthand to reduce metastasis.

Information on the role of CCN3 in cutaneous wound healing, includingskin scarring, is largely unknown. We hypothesized that CCN3, primarilydirected at CCN2, plays a critical regulatory role in the molecular andcellular events which underlie the wound healing response including scarformation/resolution. Further, we hypothesized that the ratio ofCCN3/CCN2 is critical for the balance to optimal wound healing withminimization and/or reversal of scar formation. When suboptimal,endogenous regulation or exogenous treatment can be used to modulateremodeling of the ECM for improved healing/scarring. It was alsopossible but untested, that small peptide mimics of CCN3 could alsoimprove wound healing and/or scarring in human skin. This would beeffective in impaired healing, for example diabetic skin lesions, butwould also be useful in minimizing scarring, for example post-surgeryincluding face reconstruction, breast augmentation etc., ingenetic-based severe scarring including keloids.

To test this we used a cell culture model of skin healing/scarring,which employed the use of primary human skin fibroblasts derived fromforeskins collected post circumcision. These have been used extensivelyin the past to grown in culture and treated with agents that are knownto drive wound healing and or scarring. We were also interested in arare form of skin fibrosis/scarring that can lead to systemic diseaseand death known as nephrogenic systemic fibrosis (NSF). NSF is acomplication of NMR diagnostics in renal impaired patients, wheregadolinium (GAD), a heavy metal, is used as a contrast agent, but insome cases appears to deposit in skin. Although the mechanism fordevelopment of skin fibrosis and subsequent systemic disease is not yetcompletely understood, we have developed a model that has allowedelucidation of the probable pathway to skin fibrosis (Bhagavathula, N.,M. K. Dame, M. DaSilva, W. Jenkins, M. N. Aslam, P. Perone and J. Varani(2010)). “Fibroblast response to gadolinium: role for platelet-derivedgrowth factor receptor.” Invest Radiol 45(12): 769-777). This disease ischaracterized as a hyperproliferative disease, and in our model it wasshown that PDGF produced by resident skin fibroblasts are stimulated byGAD to increase their production of PDGF which acts to induceproliferation and the increased production of MMPs, regulators of ECMbreakdown and thus turnover, including the major MMP, MMP-1. At the sametime tissue inhibitors of MMPs (TIMPs) are also affected by exposure toGAD. Last, although, fibroblasts do not appear to produce TGF-beta inresponse to GAD, tissue macrophages, part of the local immune response,are stimulated by GAD to produce increased amounts of TGF-beta. Itappears that local fibroblasts then respond to this increased TGF-betaby increasing their production of ECM, including predominantly collagentype 1.

We examined the role of CCN3 and CCNp in fibroproliferative/fibroticresponses in human dermal fibroblasts exposed to Omniscan, one of thegadolinium-based contrast agents associated with development ofnephrogenic systemic fibrosis. These studies were carried out as we havepreviously described (Riser, B. L., N. Bhagavathula, P. Perone, K.Garchow, Y. Xu, G. J. Fisher, F. Najmabadi, D. Attili and J. Varani(2012)). “Gadolinium-induced fibrosis is counter-regulated by CCN3 inhuman dermal fibroblasts: a model for potential treatment of nephrogenicsystemic fibrosis.” J Cell Commun Signal 6(2): 97-105). In our studies,human dermal fibroblasts were exposed to Omniscan; or to PDGF and TGF-β1as controls. Cellular proliferation was assessed along with MMP-1 (byELISA and gelatin zymography), TIMP-1 (by ELISA) and COL1 (by ELISA) inthe absence and presence of CCN3 and CCNp. CCN3 and CCNp38 was added tocells at 10 nM concentration and at the same time as PDGF. In parallel,CCN3 production was assessed in control and Omniscan-treated cells. Inmost case the results shown (each bar) are the mean of 3-5 separateexperiments, using fibroblasts from different donors. CCN3 was producedin our laboratory from the human embryonic kidney cell line (HEK-293)transfected with the complete human CCN3 gene, and producing anapproximate 55 kDa, full-length CCN3 product. A second source of CCN3was obtained from Pepro Tech Corporation (Rocky Hill, N.J.) and isproduced in a prokaryote cell line.

FIG. 13 demonstrates the increased human skin fibroblast proliferationin response to Omniscan (GAD). FIG. 14 shows that human skin fibroblastsproduce and secrete CCN3 in culture under basal conditions, and theexposure to GAD dose-dependently decreases this CCN3 production, whileat the same time increasing cell proliferation (compare to FIG. 13).This suggested that CCN3 is able to control fibroblast proliferation.This is important since, NSF, and certain other fibrotic diseases arecharacterized as fibroproliferative diseases. In these instancesproliferation of a key effecter cell results in the overaccumulation ofECM, i.e., collagen, and fibrosis.

Since it had been shown that skin fibroblasts also produce the cytokineplatelet derived growth factor (PDGF) in response in response to GAD,and this is the likely mediator of the increased cell proliferation(Bhagavathula, N., M. K. Dame, M. DaSilva, W. Jenkins, M. N. Aslam, P.Perone and J. Varani (2010)). “Fibroblast response to gadolinium: rolefor platelet-derived growth factor receptor.” Invest Radiol 45(12):769-777), we looked next at the response to PDGF, and the role of CCN3and CCNp. FIG. 15 demonstrates that human fibroblast proliferation isincreased by PDGF and this stimulation is blocked by the addition ofCCN3 protein and equally well by CCNp38-3 (Seq. ID. No. 56). FIG. 16shows that TGF-beta does not stimulate cell proliferation in this model,and neither CCN3 (SEQ. ID. No. 67) nor CCNp38-3 (Seq. ID. No. 56) has aneffect on baseline cell growth.

Extracellular matrix (ECM) accumulation is a dynamic process made up ofboth regulated synthesis and breakdown (ECM turnover). Accumulation oroveraccumulation in fibrosis is the result of an imbalance in the twoand can therefore be the result of increased synthesis or decreasedturnover rates. Fibrosis is often characterized by an increase in bothsynthesis and breakdown, i.e., increased turnover, and is the result ofthe net change. Matrix metalloproteinase one (MMP-1) acts to increasebreakdown, whereas tissue inhibitors of MMP (e.g., TIMPs) at least inpart to control the activity of MMP.

FIG. 17 shows that PDGF also acts to increase MMP-1 activity, whereasCCN3 is able to block that increase. CCNp38-3 (Seq. ID. No. 56) worksbetter than CCN3 protein to accomplish this blockade. FIG. 18 shows nostimulating effect of TGF-beta and therefore no effect of CCN3 or thepeptide.

FIG. 19 shows that PDGF also acts to increase TIMP-1 production andneither CCNp38-3 (Seq. ID. No. 56) nor CCN3 (SEQ. ID. No. 67) is able toblock or reduce the increase in TIMP-1 production. FIG. 20 shows thatTGF-beta1 fails to stimulate TIMP-1 production and neither CCNp38-3 norCCN3 have an effect. FIG. 21 shows that TGF-beta exposure increasespro-collagen production 2-fold or greater and both CCN3 ((SEQ. ID. No.67) and CCNp38-3 (Seq. ID. No. 56)) completely block the increase.

Collectively, these results show that CCN3 is an endogenousanti-scarring agent in the skin, and will therefore as shown beparticularly important in NSF and likely other forms of skin scarringand in organs including the skin where there is exposure to other heavymetals. CCNp38-3 (SEQ. ID. 56) will also be useful to treat suchdisorders.

Next we created and tested for efficacy, additional CCNp including thosewith the cysteines intact (native sequence) from CCNp37 and CCNp38 andthose that were modified by either shortening the peptide by 1 or 2amino acids or lengthening by one amino acid. These agents were added tohuman skin fibroblasts in increasing concentrations from 1 nM to 100 nMand compared to the equal concentration of CCN3 (SEQ. ID. NO: 67). Theywere added just prior to the addition of either TGF-beta or PDGF,depending on the experiment.

FIGS. 22-24 show the test results of the effect of modifications inCCNp37 and CCNp38 (as described) on PDGF stimulated human fibroblastproliferation at 1 nM, 10 nM, and 100 nM concentrations respectively andcompared the effect to that of CCN3, to determine their suitability astherapeutic agents.

FIG. 22 shows, human skin fibroblast proliferation in response to PDGFand the effect of 1 nM CCN3 or CCNp peptide. As expected PDGF exposureproduced a strong increase in cell proliferation. CCN3 (SEQ. ID. No. 67)alone slightly decreased proliferation whereas all of the peptides had asimilar or greater reduction (8-22%) in proliferation. FIG. 23 showshuman skin fibroblast proliferation in response to PDGF and the effectof 10 nM CCN3 or CCNp peptide. CCN3 alone produced a 33% reduction inproliferation, whereas the CCNp peptides produced a similar 19-30%inhibition. FIG. 24 shows human skin fibroblast proliferation inresponse to PDGF and the effect of 100 nM CCN3 or CCNp peptides. CCN3alone produced a 46% reduction in proliferation, whereas the CCNppeptides produced a similar 19-36% inhibition.

Taken as a whole there was a dose-dependent efficacy of CCN3 and all ofthe CCNp peptides in this tested group, although there were somedifferences in the CCNp peptides dependent on the modification. Addingan amino acid to the C-term end of CCNp 38 did not improve control ofproliferation. Shortening CCNp38 at the N-term may have reduced slightlythe ability to block proliferation. The native form of CCNp38 inhibitedproliferation stimulated by PDGF, but was not as effective as thesubstituted form. CCNp37 shortened by 2 amino acids at the N or C-termproduced cell proliferation-inhibition activity similar to the full 14mer form. The native form of CCNp37 was active in inhibitingproliferation but was slightly less effective at most concentrations.

FIGS. 25-27 show the test results of the effect of modifications inCCNp37 and CCNp38 (as described) on their ability to block PDGFstimulated MMP-1 production, as a measure of their effectiveness inblocking skin fibrosis/scarring.

In FIG. 25, CCN3 at 1 nM was able to block little or no MMP-1production, whereas all of the peptides tested in this series blockedsignificantly at 1 nM (16-44%). In FIG. 26, the effect of CCN3 at 10 nMwas increased (to 27% reduction in MMP-1), whereas the CCNp peptides insome cases increased their activity to as much as 60% inhibition. InFIG. 27 at 100 nM CCN3 reached a 30% reduction in the stimulated MMP-1production, whereas all CCNp peptides had similar or stronger activity,with CCNp38-3 and CCNp38-4 blocking up to about 60%. All peptidevariants were able to block a marked level of MMP-1 production,including those with either cysteine intact or a replacement withserine. However, when CCNp37 had the native cysteine intact, or was madeslightly shorter by reducing 2 amino acids at the N- or C-terminus, theability to block MMP-1 production was reduced at all concentrations.

For CCNp38, the mouse sequence was effective, but slightly lesseffective in these human cells than the human sequence. The nativeCCNp38 produced similar activity to the cysteine substituted sequence.Reducing 2 amino acids from the N-term end or adding 1 amino acid to theC-term end resulted in slightly lower activity, but still producedinhibition of PDGF-stimulated MMP-1 production. Because MMP-1 productionis important to ECM turnover, and other criticial biological activities,the ability of these short peptides to modify its production can beinterpreted to mean that they can be used as therapeutic agents infibrosis, cancer and other pathologies where there is either amisregulation of MMP-1, or a need to block the production of MMP-1involved in other disease, including inflammation.

FIGS. 28-30, show the test results of the same series of peptides fortheir ability to block PDGF stimulated TIMP-1 production, as a measureof their effectiveness to alter the accumulation of ECM and thus skinfibrosis/scarring, and other related disease. TIMP-1 production is knownto be associated with a reduction in ECM breakdown and thus reducedturnover and in some cases increased ECM accumulation, includingcollagen. Increased turnover may also result in misstructured, orimperfect, lower functioning, ECM. We found that unlike the case forMMP-1, CCN3 was unable to block the increase in TIMP-1 stimulated byPDGF (FIGS. 29 and 30 [not tested in FIG. 28]). As was the case forCCN3, most of the peptides were also unable to alter the production ofTIMP-1 even at the highest dose used. However, unexpectedly CCNp37-12(Seq. ID. No. 37) and CCNp38-1 (Seq. ID. No. 38) produced approximately50% and 70% reduction respectively in TIMP-1 (FIG. 30). CCNp38-3 (Seq.ID. No. 56), 38-4 (Seq. ID. No. 50), and 38-9 (Seq. ID. No. 57) weretested at the high dose only. These results demonstrate that the abilityof CCNp peptides, and CCN3 to block the stimulated production of MMP-1above (FIG. 25, 26, 27), was not likely due to their ability to increaseTIMP-1. Since, in many pathologies, the ability to heal versus theinability to heal, and to form scar or fibrosis, is the result of thebalance of ECM synthesis versus breakdown, the ability totherapeutically control this process by selectively treating with aCCN3, or specific CCNp peptide, and at the proper timing, to controlsynthesis versus breakdown, and thus the balance of turnover, will allowthe prevention of progression as well as the reversal of pathology tonormal tissue.

FIGS. 31-33 show the test results of the effect of modifications inCCNp37 and CCNp38 (as described) on TGF-beta-stimulated human fibroblastpro-collagen production and compared the effect to that of CCN3 (Seq.ID. No. 67), to determine suitability as therapeutic agents. Asexpected, TGF-beta significantly increased the production ofpro-collagen type 1 whereas CCN3 was able to block from 66% toapproximately 86% of the stimulated pro-collagen production as the dosewas increased (1-100 nM). All of the peptides tested except CCNp 37-12(Seq. ID. No. 37) were able to reduce the stimulation of pro-collagentype 1 production to some degree. CCNp38-3 (Seq. ID. No. 56) however,was as effective as CCN3 (SEQ. ID. No. 67).

Collectively, the results from FIGS. 31-33 demonstrate that CCN3 andCCNp described herein, can be used to prevent or modify the course ofhealing, scarring and fibrosis in skin in NSF and likely in other skinconditions where PDFG, TGF-beta, CCN2, MMP-1, TIMP-1, and collagen areinvolved. This is also therefore likely to be the case in other forms,and organs where impaired healing, fibrosis, or inflammation areinvolved. The selective use of CCN3 or the appropriate CCNp peptide cantherefore be used, and “custom tailored” for the patient in need. Thiswas a further unexpected discovery.

Results from DN Animal Model

In addition to the data shown in above examples, that demonstrated anability of CCNp37 and CCNp38 (SEQ. ID. 37, 38, 49, 50) in cell models ofrenal disease, this confirmation was further sought in an animal modelof human disease. FIG. 34 shows the method used to test efficacy ofpeptide CCNp38 in an animal model of diabetic renal disease. This wascarried out using the BTBR Ob/Ob mouse strain that has a defectiveleptin receptor that results in increased appetite. As a result itrapidly gains weight over the control strain and becomes hyperglycemicat about one month of age, going on to develop renal disease resemblingthat in humans. This is regarded by some to be the rodent model bestmirroring renal disease in humans as a complication of diabetes. Animalswere treated with either rCCN3 (SEQ. ID. NO: 67) or CCNp38 (SEQ. ID. NO:38) beginning at 9 weeks of age, when early renal disease has beendocumented. The disease was allowed to develop for 9 weeks, thentreatment started. Mice were treated 3 times per week for 8 weeks. At 17weeks, blood and urine were collected, and animals sacrificed with organsamples collected. The effect of treatment with either CCN3 (2concentrations, 2 or 20× the circulating amounts) or mimic peptide(CCNp38, 2 concentrations, 20 or 200× the equivalent molar circulatingconcentration of CCN3) was tested. Assays to determine the effect ofCCN3 or peptide on expression of target fibrosis genes and clinicalpathology were determined using methods as previously described (Riser,Amer J Pathology 2009) and (McIntosh, L M, et al., SelectiveCCR2-targeted macrophage depletion ameliorates experimentalmesangioproliferative glomerulonephritis, Clinical and ExperimentalImmunology, 2008, 155, 295-303).

FIG. 34 shows the method used to test efficacy of peptide CCNp38 in ananimal model of diabetic renal disease. This was carried out using theBT/BR Ob/Ob mouse strain that has a defective leptin receptor thatresults in increased appetite. As a result mice rapidly gain weight overthe control strain and become hyperglycemic at about one month of agegoing on to develop renal disease resembling that in humans. This isregarded by some to be the best rodent model for mirroring renal diseasein humans as a complication of diabetes. The lower part of FIG. 34 showsthe documented changes that occur in this mice strain, primarily focusedon the kidney. The upper part of the figure shows the comparable changesthat have been documented and are characteristic of human progression.Animals were treated with either rCCN3 (SEQ. ID. NO: 67) or CCNp38 (SEQ.ID. NO: 38) beginning at 9 weeks of age, when early renal disease hasbeen documented. Mice were treated for 8 weeks, then sacrificed andmeasured for renal disease and other complications, and the effect drugtreatment. Test animals were documented to have developed diabetes by 9weeks, and were randomized for treatment, thus providing equivalentblood glucose levels in each treated group.

FIG. 35 shows that 17 weeks of diabetes elevates plasma creatinine,substantiating renal damage, and 8 weeks of treatment with CCN3 (SEQ.ID. NO: 67) or CCNp38 (SEQ. ID. 38), reduces or blocks this pathology.FIG. 36 shows that 17 weeks of diabetes elevates the albumin tocreatinine ratio, substantiating protein leakage and renal damage, and 8weeks of treatment with CCN3 or CCNp38 greatly blocks this pathology.FIGS. 37A and B shows that 17 weeks of diabetes results in mesangialexpansion, substantiating renal fibrosis, and 8 weeks of treatment withCCN3 or CCNp38 greatly block this pathology and treats the disease. FIG.37A shows qualitatively by PAS staining, in gray scale, that 17 weeks ofdiabetes results in mesangial expansion, substantiating renal fibrosis(white stain shows collagen deposition). FIG. 37B shows quantitativelyby image analysis of multiple PAS stains (3 sections per mouse/7 miceper treatment group) that that 17 weeks of diabetes results in mesangialexpansion, substantiating renal fibrosis., and 8 weeks of treatment withCCN3 or CCNp38 greatly blocks/treats this pathology.

FIG. 38 shows that renal mRNA levels for the fibrosis gene CCN2 areincreased by diabetes, and treatment with CCN3 or CCNp38 greatly reducesor blocks the increase, thus treating the disease. FIG. 39 shows thatrenal mRNA levels for the fibrosis gene Col1A2 are increased bydiabetes, and treatment with CCN3 or CCNp38 greatly reduces or blocksthe increase, thus treating the disease. FIG. 40 shows that renal mRNAlevels for the control 18S rRNA are not increased by diabetes, andtreatment with CCN3 or CCNp38 has no effect on levels. These datademonstrate the usefulness of CCNp peptides in the treatment of renalfibrosis. They demonstrate a useful method and dose of treatment,however more or less frequent dosing and with higher or lower dose couldbe used depending on the individual patient needs and the route ofdelivery described in greater detail below.

A complication of diabetes, obesity, older age, alcohol use and otherphysiological abnormalities including metabolic syndrome is fatty liver.Accumulation of fat may also be accompanied by a progressiveinflammation of the liver (hepatitis), called steatohepatitis. Fattyliver may be termed alcoholic steatosis or nonalcoholic fatty liverdisease (NAFLD), and the more severe forms as alcoholic steatohepatitisand non-alcoholic steatohepatitis (NASH). In some cases this can lead toliver fibrosis or cirrhosis, one of the leading causes of death indiabetic patients. Liver cancer is rare, but does not appear to occurwithout first having liver fibrosis. CCN2 has been shown to be increasedin liver fibrosis and liver cancer, and has been shown to be causal incertain animal models of liver fibrosis (Connective tissue growth factor(CCN2, CTGF) and organ fibrosis: lessons from transgenic animals, D RBrigstock—Journal of cell communication and signaling, 2010—Springer)(Connective tissue growth factor: a fibrogenic master switch in fibroticliver disease, Olav A. Gressner, Axel M. Gressner, Liver International,first published online: 6 Aug. 2008, 1478-3231).

Since a common complication of diabetes is fatty liver, hepatitis, NASH,and in some cases liver fibrosis, we used the BTBR Ob/Ob mouseexperiments described above as a model of human liver disease to examinethe possibility that CCN3 or more particularly CCNp peptides mightprovide a treatment to prevent, treat, or reverse the liver diseasedescribed above.

FIG. 41 shows that liver weight is greatly increased by 13 weeks ofobesity and diabetes, demonstrating steatosis. Treatment with for 8weeks with CCN3 or CCNp38 slightly reduces this increase. FIG. 42 showsthat liver mRNA levels for the fibrosis gene CCN2 are increased bydiabetes, substantiating an inflammatory response and initiation ofliver hepatitis/fibrosis. Treatment with CCNp38 dose-dependently reducedthe increase. FIG. 44 shows that liver mRNA levels for the fibrosis geneCol1A2 are increased by diabetes, substantiating the initiation offibrosis. Treatment with CCN3 or CCNp38 dose-dependently reduced, orblocked the increase in collagen expression. This demonstratesusefulness for CCN3, but more effectively, CCNp peptides for treatingsteatosis, hepatitis, liver fibrosis, and prevention of liver cancer.

A common type of cardiac disease is fibrosis. This can occur in theheart muscle itself, the valves of the heart, and/or the coronaryarteries. It can be a slow progressive disease associated withinflammation and/or fatty diet, or can result from acute event includingmyocardial infarction (MI). It is a common complication of chronickidney disease and diabetes. Another form of heart disease is cardiachypertrophy. This can be associated with genetic alteration or canresult from injury or overload to the heart and is also associated withfibrosis. CCN2 is upregulated and thought to be an important causalfactor in the development of cardiac fibrosis and cardiac hypertrophy(Wang, Xiaoyu, et al. “Adverse effects of high glucose and free fattyacid on cardiornyocytes are mediated by connective tissue growthfactor.” American Journal of Physiology-Cell Physiology 297.6 (2009):C1490-C1500), (Connective tissue growth factor and cardiac fibrosis, A.Daniels¹, M. Van Bilsen¹, R. Goldschmeding², G. J. Van Der Vusse¹, F. A.Van Nieuwenhoven¹. Acta Physiologica Article first published online: 27Nov. 2008, 1748-1716).

A second important molecule in cardiac fibrosis is PAI. PAI-1 has beenshown to be increased post MI and also following other forms of injuryin the heart associated with fibrosis. Studies in PAI-1 deficient micehave shown that this deficiency protects against fibrosis (PAI-1 inTissue Fibrosis, Asish K. Ghosh and Douglas E. Vaughan, J. Cell.Physiol. 227: 493-507, 2012.)

The BTBR Ob/Ob mouse was used to model human cardiac disease associatedwith diabetes and also chronic renal disease, to determine efficacy ofCCN3 and CCNp peptides on the development of cardiac changes associatedwith diabetes, including cardiac fibrosis. We examined the heart fromthe same set of experiments as describe above for the kidney. FIG. 44shows that heart mRNA levels for the fibrosis gene plasminogen activatorinhibitor 1 (PAI-1) a target pro-fibrotic gene is increased by diabetes,substantiating the initiation of fibrosis. Treatment with CCNp38 greatlyreduces, and at the high dose blocks the increase. Since CCNp has beenshown to inhibit the production and activity of CCN2 and it has beenshown here to block the increase in PAI-1 in the heart of diabetic miceassociated with fibrosis, it can be used as a preventative or treatmentfor cardiac fibrosis, not limited to, but including those associatedwith diabetes, chronic kidney disease, atherosclerosis, vascularcalcification, and hypertrophy. This can be further proven, for exampleby using a mouse model of familial hypertrophic cardiomyopathy (SevereHeart Failure and Early Mortality in a Double-Mutation Mouse Model ofFamilial Hypertrophic Cardiomyopathy, Tatiana Tsoutsman, Matthew Kelly,Dominic C. H. Ng, PhD; Ju-En Tan, Emily Tu, Lien Lam, Marie A.Bogoyevitch, Christine E. Seidman, J. G. Seidman, Christopher Semsarian,Circulation. 2008; 117:1820-1831). In this case, CCN3 or CCNp peptideswould be administered beginning at birth, by preferably IV, IP oranother route. In some groups, the agent described would be administeredshortly after the established development of cardiac hypertrophy.Treatment could be extended to about 21 days, then heart collected andexamined for reduction in cardiac pathology (including measurement byhistopathology). Measurements of dilated cardiomyopathy and heartfailure, and level of ventricular arrhythmias, and blood biomarkers ofcardiac disease would also be run to demonstrate efficacy of the agent.In one set of experiments the end point measured would be reduction inmortality.

Sustained neuroinflammation strongly contributes to the pathogenesis ofpain. The clinical challenge of chronic pain relief has demonstrated arole for molecules including CCN3 and MMP-1 among others. It hasrecently been shown that CCN3 is a modulator of these inflammatorymediators in a preclinical model of persistent inflammatory pain. Theyshowed that in this model that injury with neuroinflammation results inthe downregulation of CCN3 in nerves. Intrathecal treatment specificallyabolished the induction of MMP-2 and other modulators of inflammationand pain in rats. This inhibitory effect on MMP is associated withreduced pain on mechanical stimulation (NOV/CCN3 attenuates inflammatorypain through regulation of matrix metalloproteinases-2 and -9, LaraKular, Cyril Rivat, Brigitte Lelongt, Claire Calmel, Maryvonne Laurent,Michel Pohl, Patrick Kitabgi, Stéphane Melik-Parsadaniantz and CécileMartinerie. Journal of Neuroinflammation, 2012, 9:36). Accordingly,since CCNp peptides described herein have been demonstrated to mimic theability of CCN3, and to reduce stimulated MMP production, then CCNp37and CCnp38 and their variants can be used to treat neuroinflammation andpain. This could be further proven in two types of experiments the firstin rats to which Freund's adjuvant (CFA) is given to induce a model ofpersistent inflammatory pain (same reference as above). CCNp37 andCCNp38 and combinations would then be administered intrathecally orother, beginning before the CFA, to show efficacy for prevention, orbeginning after developed neuroinflammation to demonstrate efficacy oftreatment. The second method would use cultured primary sensory neuronsfor in vitro experiments (same reference) and CCNp peptides tested toshow an ability to block IL-1b- and TNF-α-induced MMP-2, MMP-9 and CCL2expression, as a model for human neuroinflammation and pain.

As an additional aspect, the invention includes kits which comprise oneor more pharmaceutical formulations for administration of CCN3 peptidesto a patient packaged in a manner which facilitates their use foradministration to subjects. In one embodiment, such a kit includespharmaceutical formulation described herein (e.g., a compositioncomprising a CCN3 protein or a CCNp peptide), packaged in a containersuch as a sealed bottle or vessel, with a label affixed to the containeror included in the package that describes use of the compound orcomposition in practicing the method. In one embodiment, thepharmaceutical formulation is packaged in the container such that theamount of headspace in the container (e.g., the amount of air betweenthe liquid formulation and the top of the container) is very small.Preferably, the amount of headspace is negligible (i.e., almost none).In one embodiment, the kit contains a first container having the CCNppeptide composition and a second container having a physiologicallyacceptable reconstitution solution for the composition. In one aspect,the pharmaceutical formulation is packaged in a unit dosage form. Thekit may further include a device suitable for administering thepharmaceutical formulation according to a specific route ofadministration. Preferably, the kit contains a label that describes useof the pharmaceutical formulations.

The present invention further provides administering the CCNp peptidesto a human subject through a route of administration includingintravenous, intramuscular, nasal, topical, vaginal, anal, transdermal,inhalation, oral, bucal, intraperitoneal, intraosseous and combinationsof the same. The transdermal route of administration includestransdermal patch or transdermal electrophoresis. It should also beunderstood that the CCNp peptide can be modified by attaching a carriermolecule or entity, as is well known in the art, to protect the peptidefrom degradation, to target the peptide to a desired location in thehuman, and to control the rate of delivery. Suitable carrier moleculesinclude, but are not limited to, glycol groups, polyethylene glycol(PEG), proteins, including serum proteins. The present inventioncontemplates using excipients that are used in the pharmaceuticalindustry for the prescribed routes of delivery set forth above. Thepresent invention contemplates modifying the CCN3 peptide to increaseits stability, shelf life, half-life in vivo, targeting within the body,to improve its attachment to a cell of interest or entry into the cellof interest.

In one preferred form of the invention, the CCNp peptides can be used instem cell treatment formulations by adding the peptides to cord blood,or bone marrow isolates to generate therapeutic stem cells ex vivo.Also, it could be speculated that such treatment in vivo might enhancethe activity of naturally occurring stem cells, for better recovery fromserious injury including ischemic heart disease, fibrosis, heart andliver failure among others. Hematopoietic stem cells (HSC) would beobtained from a patient (or donor) e.g., including bone marrow,peripheral blood, and umbilical cord blood cells, including autologous(marrow or PBSC) or allogeneic (HLA-matched related [MRD], HLA-matchedunrelated [MUD], mismatched related or unrelated donors, and umbilicalcord blood [UCB] or form an established stem cell line). These stemcells would then be incubated for a period of time in the presence ofCCN3 or CCNp peptides, described herein, to allow growth (expansion ofnumbers) and/or differentiation to the needed cell type or form. Theconditioned stem cell would then be delivered to a patient, e.g., IV orother route of administration described herein, with a given pathologyincluding but not limited to fibrosis, cancer, multiple sclerosis,cystic fibrosis in order to target to the site of injury and pathology.The conditioned stem cells would serve to: 1) replace specificallyinjured or dead cells at the site of pathology (e.g. cardiac musclecells, kidney mesangial cells, liver stellate cells) and 2) to provideaccessory cells differentiated and capable of releasing cytokines andother factors necessary for repair or replacement.

The present invention provides for delivering an effective amount of theCCN3 peptides which can be determined by methods such as dose titrationor other techniques known to those skilled in the art and can includedosages within the range of 0.1 nanomolar to 1 micromolar orapproximately 0.1 nanogram per milliter to 1 microgram per milliliter.Concentrated amounts may also be required depending on the delivery formused.

The practice of the present invention will employ and incorporate,unless otherwise indicated, conventional techniques of cell biology,cell culture, molecular biology, microbiology, genetic engineering andimmunology, which are within the skill of the art. While the presentinvention is described in connection with what is presently consideredto be the most practical and preferred embodiments, it should beappreciated that the invention is not limited to the disclosedembodiments, and is intended to cover various modifications andequivalent arrangements included within the spirit and scope of theclaims. Modifications and variations in the present invention may bemade without departing from the novel aspects of the invention asdefined in the claims. The appended claims should be construed broadlyand in a manner consistent with the spirit and the scope of theinvention herein.

The invention claimed is:
 1. A CCN3 peptide comprising a sequenceselected from the group consisting of SEQ ID NOs: 36, 37, 38, 42, 49,50, 53, 54, 55, 56, 57, 58, and
 60. 2. A method for treating fatty liverdisease, steatosis, liver fibrosis, liver cancer, hepatitis,inflammation, or neural inflammation in a subject comprising:administering to the subject an effective amount of a CCN3 peptidecomprising a sequence selected from the group consisting of SEQ ID Nos:36-38, 40, 42, 49-50, 53-58, 60, and combinations thereof.
 3. The methodof claim 2 wherein the step of administering comprises deliveringthrough a route of administration selected from the group consisting ofintravenous, intramuscular, nasal, topical, vaginal, anal, transdermal,inhalation, oral, buccal, intraperitoneal, intrathecal, intraosseous andcombinations thereof.
 4. The method of claim 3 wherein the transdermalroute of administration is transdermal patch or transdermalelectrophoresis.
 5. The method of claim 2 further comprisingadministration of a carrier molecule.
 6. The method of claim 5 whereinthe carrier molecule is selected from the group consisting of:polyethylene glycol (PEG), glycol groups, proteins, and serum proteins.7. The method of claim 2, wherein the method further comprisesadministering a stem cell solution.